Resource Centre
Publication )
Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillars
Publication )
Feasibility of long-read nanopore sequencing for methylation-based classification of posterior fossa ependymomas
Workflow Workflow overview: Hereditary Cancer Panel
Publication )
Long-read genome sequencing enhances diagnostics of paediatric neurological disorders
Video )
AMP 2025: Rapid comprehensive molecular profiling of CNS tumors
Video )
AMP 2025: Oxford Nanopore-based structural and epigenetic profiling of D4Z4 arrays in FSHD
Video )
AMP 2025: Long-range PCR meets long-read sequencing to resolve challenging ACMG tier 3 carrier screening genes
Video )
AMP 2025: Epigenomic diagnosis and prognosis of Acute Myeloid Leukemia
Publication )
RAPID: a targeted long-read RNA workflow for functional resolution of splicing variants in rare disease
Knowledge exchange )
Fast answers and the most complete view: 24-hour whole-genome sequencing with Oxford Nanopore
Webinar )
Transforming hereditary cancer sequencing with adaptive sampling target enrichment
Publication )
Proof-of-principle: Nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid alleles
Video )
cfDNA methylation sequencing: a precision tool for early detection of neurodegenerative disorders
Publication ![Oxford Nanopore Technologies [ONT] sequencing: clinical validation in genetically heterogeneous disorders](https://a.storyblok.com/f/196663/94b60f6ad1/low-resolution-png-dna_wide_highres_1-16-1_1.png/m/700x470/filters:format(webp))
Oxford Nanopore Technologies [ONT] sequencing: clinical validation in genetically heterogeneous disorders
Publication )
Ensilication preserves high-molecular-weight native DNA for clinical long-read sequencing
Video )
Sequencing from large scale to single cell — the new era of biological discovery
Video )
Enhanced hereditary cancer screening through scalable parent-of-origin-aware genomic analysis
Poster Resolving challenging medically-relevant genes using nanopore sequencing
Poster )
A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing
Poster )
Comprehensive resolution of challenging genomic variation with Oxford Nanopore telomere-to-telomere assemblies